The E3 ubiquitin ligase Itch in T cell activation, differentiation, and tolerance

被引:50
作者
Liu, Yun-Cai [1 ]
机构
[1] La Jolla Inst Allergy & Immunol, Div Cell Biol, La Jolla, CA 92037 USA
关键词
itch; ubiquitin; E3; ligase; T helper type 2; Jun proteins; anergy; asthma;
D O I
10.1016/j.smim.2007.02.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tagging a small molecule ubiquitin to a protein substrate, or protein ubiquitination, plays an important role in the immune responses. This process is catalyzed by a cascade of enzymatic reactions, with the E3 ubiquitin ligases being the critical enzymes that determine the specificity of substrate recognition. The E3 ligase Itch was identified from a mutant mouse which displays skin scratching and abnormal immune disorders. In the past few years, much progress has been made in our understanding of Itch-promoted protein ubiquitination, modulation of its ligase activity by upstream kinases, and the kinase-ligase interaction in T cell differentiation and tolerance induction. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:197 / 205
页数:9
相关论文
共 83 条
[1]   GRAIL:: An E3 ubiquitin ligase that inhibits cytokine gene transcription is expressed in anergic CD4+ T cells [J].
Anandasabapathy, N ;
Ford, GS ;
Bloom, D ;
Holness, C ;
Paragas, V ;
Seroogy, C ;
Skrenta, H ;
Hollenhorst, M ;
Fathman, CG ;
Soares, L .
IMMUNITY, 2003, 18 (04) :535-547
[2]   Projection of an immunological self shadow within the thymus by the aire protein [J].
Anderson, MS ;
Venanzi, ES ;
Klein, L ;
Chen, ZB ;
Berzins, SP ;
Turley, SJ ;
von Boehmer, H ;
Bronson, R ;
Dierich, A ;
Benoist, C ;
Mathis, D .
SCIENCE, 2002, 298 (5597) :1395-1401
[3]   The HECT domain ligase itch ubiquitinates endophilin and localizes to the trans-Golgi network and endosomal system [J].
Angers, A ;
Ramjaun, AR ;
McPherson, PS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (12) :11471-11479
[4]   Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[5]   Negative regulation of lymphocyte activation and autoimmunity by the molecular adaptor Cbl-b [J].
Bachmaier, K ;
Krawczyk, C ;
Kozieradzki, I ;
Kong, YY ;
Sasaki, T ;
Oliveira-dos-Santos, A ;
Mariathasan, S ;
Bouchard, D ;
Wakeham, A ;
Itie, A ;
Le, J ;
Ohashi, PS ;
Sarosi, I ;
Nishina, H ;
Lipkowitz, S ;
Penninger, JM .
NATURE, 2000, 403 (6766) :211-216
[6]   Itch E3 ligase-mediated regulation of TGF-β signaling by modulating Smad2 phosphorylation [J].
Bai, YL ;
Yang, C ;
Hu, K ;
Elly, C ;
Liu, YC .
MOLECULAR CELL, 2004, 15 (05) :825-831
[7]   The C2 domain of PKCδ is a phosphotyrosine binding domain [J].
Benes, CH ;
Wu, N ;
Elia, AEH ;
Dharia, T ;
Cantley, LC ;
Soltoff, SP .
CELL, 2005, 121 (02) :271-280
[8]   Natural versus adaptive regulatory T cells [J].
Bluestone, JA ;
Abbas, AK .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (03) :253-257
[9]   SAP regulates TH2 differentiation and PKC-θ-mediated activation of NF-κB1 [J].
Cannons, JL ;
Yu, LJ ;
Hill, B ;
Mijares, LA ;
Dombroski, D ;
Nichols, KE ;
Antonellis, A ;
Koretzky, GA ;
Gardner, K ;
Schwartzberg, PL .
IMMUNITY, 2004, 21 (05) :693-706
[10]   The E3 ubiquitin ligase itch couples JNK activation to TNFα-induced cell death by inducing c-FLIPL turnover [J].
Chang, LF ;
Kamata, H ;
Solinas, G ;
Luo, JL ;
Maeda, S ;
Venuprasad, K ;
Liu, YC ;
Karin, M .
CELL, 2006, 124 (03) :601-613